Canonical Allele Identifier: CA98667357
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1049238675
gnomAD v3: 4-67740132-G-GT
gnomAD v4: 4-67740132-G-GT
MyVariant Identifiers: chr4:g.68605850_68605851insT (hg19) chr4:g.67740132_67740133insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740139dup , CM000666.2:g.67740139dup GRCh38
NC_000004.11:g.68605857dup , CM000666.1:g.68605857dup GRCh37
NC_000004.10:g.68288452dup NCBI36
NG_009293.1:g.20954dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*347dup MANE Select ENSP00000226413.5:n.*347dup
ENST00000226413.4:c.*347dup ENSP00000226413.4:n.*347dup
NM_000406.2:c.*347dup NP_000397.1:n.*347dup
NM_001012763.1:c.*456dup NP_001012781.1:n.*456dup
NM_000406.3:c.*347dup MANE Select NP_000397.1:n.*347dup
NM_001012763.2:c.*456dup NP_001012781.1:n.*456dup
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